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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/72651
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dc.contributor.authorPhilip J. Chevisen_US
dc.contributor.authorThanika Promchaien_US
dc.contributor.authorChristopher Richardsonen_US
dc.contributor.authorThunwadee Limtharakulen_US
dc.contributor.authorStephen G. Pyneen_US
dc.date.accessioned2022-05-27T08:27:34Z-
dc.date.available2022-05-27T08:27:34Z-
dc.date.issued2022-02-14en_US
dc.identifier.issn1364548Xen_US
dc.identifier.issn13597345en_US
dc.identifier.other2-s2.0-85124498777en_US
dc.identifier.other10.1039/d1cc06775cen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124498777&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/72651-
dc.description.abstractA highly diastereoselective method for the synthesis of syn-β-amino alcohols and enantioenriched anti-β-amino alcohols has been developed involving α-hydroxyl aldehydes and chiral α-phenylaminoxyaldehydes or α-benzoyloxyaldehydes, respectively in Petasis borono-Mannich allylation reactions. This study broadens the scope and utility of the Petasis reaction to include pinacol allylboronate and highlights its unique reactivity and stereochemical outcomes.en_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.titleSynthesis of syn-and enantioenriched anti-β-amino alcohols by highly diastereoselective borono-Mannich allylation reactionsen_US
dc.typeJournalen_US
article.title.sourcetitleChemical Communicationsen_US
article.volume58en_US
article.stream.affiliationsUniversity of Wollongongen_US
article.stream.affiliationsChiang Mai Universityen_US
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